FDA UDI In Commercial Distribution 🇺🇸 United States

Q-Switched Stellar M22™ Nd:YAG UP Kit

DI: 07290117770177 · Model: Q-Switched Stellar M22™ Nd:YAG UP Kit · LUMENIS BE LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Q-Switched Stellar M22™ Nd:YAG UP Kit
Primary DI
07290117770177
Version / Model
Q-Switched Stellar M22™ Nd:YAG UP Kit
Company Name
LUMENIS BE LTD
Labeler DUNS
600763501
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-02
Public Version
1
Public Version Date
2023-08-10
Public Version Status
New
Public Device Record Key
7368cd4f-9321-480c-ad65-0dd3d74b1121

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
45220 Multi-modality skin surface treatment system

Identifiers

Type ID
Primary 07290117770177

Premarket Submissions

Submission Number Supplement Number
K193500 000